These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

211 related articles for article (PubMed ID: 20162868)

  • 41. Molecular characterization of a new patient with a non-recurrent inv dup del 2q and review of the mechanisms for this rearrangement.
    Vera-Carbonell A; López-Expósito I; Bafalliu JA; Ballesta-Martínez M; Glóver G; Llópis C; Moya-Quiles R; Suela J; Fernández A; Guillén-Navarro E
    Am J Med Genet A; 2010 Oct; 152A(10):2670-80. PubMed ID: 20799321
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer.
    Kloth JN; Oosting J; van Wezel T; Szuhai K; Knijnenburg J; Gorter A; Kenter GG; Fleuren GJ; Jordanova ES
    BMC Genomics; 2007 Feb; 8():53. PubMed ID: 17311676
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Detection of a rare de novo 18p terminal deletion with inverted duplication in a Chinese pregnant woman.
    Zhu J; Qi H; Cao S; Cai L; Wen X; Tang G; Wan Q; Chen C; Wang J; Zeng W; Luo Y
    Mol Genet Genomic Med; 2019 Sep; 7(9):e868. PubMed ID: 31317671
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Deletion mapping of chromosome 8p in prostate cancer by fluorescence in situ hybridization.
    Matsuyama H; Pan Y; Skoog L; Tribukait B; Naito K; Ekman P; Lichter P; Bergerheim US
    Oncogene; 1994 Oct; 9(10):3071-6. PubMed ID: 8084616
    [TBL] [Abstract][Full Text] [Related]  

  • 45. A case of inv dup(8p) with early onset breast cancer.
    Seltmann M; Harrington P; Ponder BA
    J Med Genet; 2000 Jan; 37(1):70-1. PubMed ID: 10691415
    [No Abstract]   [Full Text] [Related]  

  • 46. 17p11.2p12 triplication and del(17)q11.2q12 in a severely affected child with dup(17)p11.2p12 syndrome.
    Girirajan S; Williams S; Garbern J; Nowak N; Hatchwell E; Elsea S
    Clin Genet; 2007 Jul; 72(1):47-58. PubMed ID: 17594399
    [TBL] [Abstract][Full Text] [Related]  

  • 47. D8S7 is consistently deleted in inverted duplications of the short arm of chromosome 8 (inv dup 8p).
    Minelli A; Floridia G; Rossi E; Clementi M; Tenconi R; Camurri L; Bernardi F; Hoeller H; Previde Re C; Maraschio P
    Hum Genet; 1993 Oct; 92(4):391-6. PubMed ID: 7901142
    [TBL] [Abstract][Full Text] [Related]  

  • 48. dup(8p)/del(8q) recombinant chromosome in a girl with hepatic focal nodular hyperplasia.
    Tokutomi T; Hayashi S; Imai K; Chida A; Ishiwata T; Asano Y; Inazawa J; Nonoyama S
    Am J Med Genet A; 2007 Jun; 143A(12):1334-7. PubMed ID: 17506094
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Fluorescence in situ hybridization evaluation of chromosome deletion patterns in prostate cancer.
    Huang SF; Xiao S; Renshaw AA; Loughlin KR; Hudson TJ; Fletcher JA
    Am J Pathol; 1996 Nov; 149(5):1565-73. PubMed ID: 8909246
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Meiotic segregation analysis in spermatozoa of pericentric inversion carriers using fluorescence in-situ hybridization.
    Morel F; Laudier B; Guérif F; Couet ML; Royère D; Roux C; Bresson JL; Amice V; De Braekeleer M; Douet-Guilbert N
    Hum Reprod; 2007 Jan; 22(1):136-41. PubMed ID: 16917123
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Prenatal exclusion of segmental trisomy in familial chromosome 21 pericentric inversion by fluorescence in situ hybridization.
    Tardy EP; Tóth A; Kosztolányi G
    Prenat Diagn; 1997 Sep; 17(9):871-3. PubMed ID: 9316133
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Inverted duplications: how many of them are mosaic?
    Pramparo T; Giglio S; Gregato G; de Gregori M; Patricelli MG; Ciccone R; Scappaticci S; Mannino G; Lombardi C; Pirola B; Giorda R; Rocchi M; Zuffardi O
    Eur J Hum Genet; 2004 Sep; 12(9):713-7. PubMed ID: 15266302
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Distal 8p deletion (8)(p23.1): an easily missed chromosomal abnormality that may be associated with congenital heart defect and mental retardation.
    Wu BL; Schneider GH; Sabatino DE; Bozovic LZ; Cao B; Korf BR
    Am J Med Genet; 1996 Mar; 62(1):77-83. PubMed ID: 8779331
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Inverted duplication of chromosome 5p14p15.3 confirmed with in situ hybridization.
    Zenger-Hain JL; Van Dyke DL; Wiktor A; Walker H; Feldman GL
    Am J Med Genet; 1993 Dec; 47(8):1198-201. PubMed ID: 8291556
    [TBL] [Abstract][Full Text] [Related]  

  • 55. [A dual-color fluorescence in situ hybridization study on the detection of inv(16) in acute myeloid leukemia].
    Li M; Xue YQ; Wu YF; Pan JL; Yao L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Aug; 20(4):331-5. PubMed ID: 12903046
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Tandem duplication/deletion in a maternally derived chromosome 9 supernumerary derivative resulting in 9p trisomy and partial 9q tetrasomy.
    Wyandt HE; Lebo RV; Fenerci EY; Sadhu DN; Milunsky JM
    Am J Med Genet; 2000 Aug; 93(4):305-12. PubMed ID: 10946358
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Rare interstitial deletion (2)(p11.2p13) in a child with pericentric inversion (2)(p11.2q13) of paternal origin.
    Lacbawan FL; White BJ; Anguiano A; Rigdon DT; Ball KD; Bromage GB; Yang X; DiFazio MP; Levin SW
    Am J Med Genet; 1999 Nov; 87(2):139-42. PubMed ID: 10533028
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Inverted duplications deletions: underdiagnosed rearrangements??
    Zuffardi O; Bonaglia M; Ciccone R; Giorda R
    Clin Genet; 2009 Jun; 75(6):505-13. PubMed ID: 19508415
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Four new cases of inverted terminal duplication: a modified hypothesis of mechanism of origin.
    Hoo JJ; Chao M; Szego K; Rauer M; Echiverri SC; Harris C
    Am J Med Genet; 1995 Sep; 58(4):299-304. PubMed ID: 8533837
    [TBL] [Abstract][Full Text] [Related]  

  • 60. The involvement of U-type dicentric chromosomes in the formation of terminal deletions with or without adjacent inverted duplications.
    Kato T; Inagaki H; Miyai S; Suzuki F; Naru Y; Shinkai Y; Kato A; Kanyama K; Mizuno S; Muramatsu Y; Yamamoto T; Shinya M; Tazaki Y; Hiwatashi S; Ikeda T; Ozaki M; Kurahashi H
    Hum Genet; 2020 Nov; 139(11):1417-1427. PubMed ID: 32488466
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.